84954-93-8 Usage
Description
ROSARIN, a compound with potential health benefits, is known for its preventative effects on belomycin-induced pulmonary fibrosis in rats and chronic obstructive pulmonary disease. It is also utilized in High Performance Thin-Layer Chromatography and NMR spectroscopy for its analytical properties.
Uses
Used in Pharmaceutical Applications:
ROSARIN is used as a preventative agent for [application reason], specifically targeting belomycin-induced pulmonary fibrosis in rats and chronic obstructive pulmonary disease. Its protective effects make it a valuable candidate for further research and potential therapeutic development.
Used in Analytical Chemistry:
In the field of analytical chemistry, ROSARIN is used as a reagent in High Performance Thin-Layer Chromatography (HPTLC) and Nuclear Magnetic Resonance (NMR) spectroscopy. Its properties allow for accurate and efficient analysis in these techniques, contributing to the advancement of chemical research and understanding.
Check Digit Verification of cas no
The CAS Registry Mumber 84954-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,5 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84954-93:
(7*8)+(6*4)+(5*9)+(4*5)+(3*4)+(2*9)+(1*3)=178
178 % 10 = 8
So 84954-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O10/c21-9-12-14(22)17(25)20(29-12)28-10-13-15(23)16(24)18(26)19(30-13)27-8-4-7-11-5-2-1-3-6-11/h1-7,12-26H,8-10H2/b7-4+/t12-,13+,14-,15+,16-,17+,18+,19+,20+/m0/s1
84954-93-8Relevant articles and documents
Synthetic method of rhodiola rosea active ingredient rosavin or rosarin
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, (2020/01/03)
The present invention provides a synthetic method of rhodiola rosea active ingredient rosavin or rosarin. A convergent synthetic strategy is adopted, rosin is used as a starting material and modifiedinto sugar acceptors through protection and deprotection strategies, then sugar acceptors and sugar donors formed by arabinopyranose and arabinyl furanose in presence of an accelerator quickly and efficiently conduct synthesis of rosavin and rosarin. The related synthetic method is cheap and easy-to-obtain in raw materials and mild in reaction conditions, the obtained product is high in purity, and compared with currently reported linear synthesis strategy, the method has very good industrialization prospects.